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Results 1 to 25 of 75113

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THE QUANTITATIVE ANALYSIS OF POLYMORPHISM ON HUMAN CHROMOSOMES 1,9,16, AND Y. IV: HETEROGENEITY OF A NORMAL POPULATIONPODUGOLNIKOVA OA; KOROSTELEV AP.1980; HUM. GENET.; DEU; DA. 1980; VOL. 54; NO 2; PP. 163-169; BIBL. 11 REF.Article

VARIABILITE DES REGIONS HETEROCHROMATIQUES DES CHROMOSOMES HUMAINS 1, 9, 16 ET YPODUGOL'NIKOVA OA; SUSHANLO KH M; PARFENOVA IV et al.1980; GENETIKA; SUN; DA. 1980; VOL. 16; NO 4; PP. 720-726; H.T. 1; ABS. ENG; BIBL. 23 REF.Article

REPORT OF THE COMMITTEE ON THE GENETIC CONSTITUTION OF CHROMOSOMES 13 TO 22FERGUSON SMITH MA; WESTERVELD A.1978; CYTOGENET. CELL GENET.; CHE; DA. 1978; VOL. 22; NO 1-6; PP. 111-123; BIBL. 6 P.Conference Paper

AUTOSOMAL CHROMOSOME ABERRATIONS. A REVIEW OF THE CLINICAL SYNDROMES CAUSED BY STRUCTURAL CHROMOSOME ABERRATIONS, MOSAIC-TRISOMIES 8 AND 9, AND TRIPLOIDY.SCHINZEL A.1976; ERGEBN. INNEREN MED. KINDERHEILKDE; DTSCH.; DA. 1976; VOL. 38; PP. 37-94; BIBL. 9 P. 1/2Article

LATERAL ASYMMETRY IN HUMAN CHROMOSOMES 1, 3, 4, 15, AND 16BRITO BABAPULLE V.1981; CYTOGENET. CELL GENET.; ISSN 0301-0171; CHE; DA. 1981; VOL. 29; NO 4; PP. 198-202; BIBL. 16 REF.Article

LATERAL ASYMMETRY IN HUMAN CONSTITUTIVE HETEROCHROMATIN: FREQUENCY AND INHERITANCE.ANGELL RR; JACOBS PA.1978; AMER. J. HUM. GENET.; U.S.A.; DA. 1978; VOL. 30; NO 2; PP. 144-152; BIBL. 9 REF.Article

GENETIC MAPPING: CHROMOSOMES 6-22KEATS B.1982; AM. J. HUM. GENET.; ISSN 0002-9297; USA; DA. 1982; VOL. 34; NO 5; PP. 730-742; BIBL. 39 REF.Article

HUMAN RING CHROMOSOMES: A REPORT OF FIVE CASESPICCIANO DJ; BERLIN CM; DAVENPORT SLH et al.1972; SEM. HOP., ANN. GENET.; FR.; DA. 1972; VOL. 15; NO 4; PP. 241-247; ABS. FR.; BIBL. 12REF.Serial Issue

VARIABILITE DE LA TAILLE DES BANDES C DES CHROMOSOMES 1, 9, 16 ET Y CHEZ L'HOMMEPODUGOL'NIKOVA OA; SYCHEVA ZH L; PROKOF'EVA BEL'GOVSKAYA AA et al.1979; CITOLOGIJA; SUN; DA. 1979; VOL. 21; NO 6; PP. 667-670; H.T. 1; ABS. ENG; BIBL. 1 P.Article

IDENTIFICATION BY FLUORESCENCE OF TWO G RINGS: (46XY, 21R) G DELETION SYNDROME I AND (46, XX, 22R) G DELETION SYNDROME IIMAGENIS RE; ARMENDARES S; HECHT F et al.1972; SEM. HOP., ANN. GENET.; FR.; DA. 1972; VOL. 15; NO 4; PP. 265-266; ABS. FR.Serial Issue

RASSEGNA DI SETTE CASI DI PATOLOGIA AUTOSOMICA DI PUI RARO RISCONTRO: TRISOMIE 9P, MONOSOMIE 18Q, ANNEAU 21, TRISOMIE 6P, TRISOMIE 2Q, TRANSLOCATION 1;21 = REVUE DE 7 CAS DE PATHOLOGIE AUTOSOMIQUE RARE: TRISOMIE 9P, MONOSOMIE 18Q, ANNEAU 21, TRISOMIE 6P, TRISOMIE 2Q, TRANSLOCATION 1:21FIORETTI G; PAGANO L; RENDA S et al.1980; MINERVA PEDIATR.; ISSN 0026-4946; ITA; DA. 1980; VOL. 32; NO 12; PP. 807-814; ABS. ENG; BIBL. 4 REF.Article

TRANSLOCATIONS APPAREMMENT EQUILIBREES A PHENOTYPE ANORMALTAILLEMITE JL; PORTNOI MF; VAN DEN AKKER J et al.1978; J. GYNECOL. OBSTETR. BIOL. REPROD.; FRA; DA. 1978; VOL. 7; NO 3; PP. 407-417; ABS. ENG; BIBL. 17 REF.Article

MEIOTIC BEHAVIOR OF FIVE HUMAN RECIPROCAL TRANSLOCATIONS.CHANDLEY AC; SEUANEZ H; FLETCHER JM et al.1976; CYTOGENET. CELL GENET.; SWITZ.; DA. 1976; VOL. 17; NO 2; PP. 98-111; BIBL. 20 REF.Article

HETEROCHROMATIC REGIONS ON CHROMOSOMES 1,9, 16, AND Y IN CHILDREN WITH SOME DISTURBANCES OCCURING DURING EMBRYO DEVELOPMENTPODUGOLNIKOVA OA; BLUMINA MG.1983; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1983; VOL. 63; NO 2; PP. 183-188; BIBL. 28 REF.Article

COMPLEX PH TRANSLOCATION IN CHRONIC MYELOID LEUKEMIAKESSOUS A; COLOMBIES P; SUDRIES M et al.1980; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1980; VOL. 2; NO 4; PP. 335-337; BIBL. 10 REF.Article

UN CAS D'ABERRATION CHROMOSOMIQUE COMPLEXE MOSAIQUE 47XY+13/48XYY+9VERGET RC; TERRIBILE A; NOEL B et al.1981; PEDIATRIE; ISSN 0031-4021; FRA; DA. 1981; VOL. 36; NO 5; PP. 387-391; ABS. ENG; BIBL. 7 REF.Article

ANALYSE COMPAREE DU POLYMORPHISME DES REGIONS HETEROCHROMATIQUES DES CHROMOSOMES 1,9,16 ET Y CHEZ DES ENFANTS NORMAUX ET ARRIERES MENTAUX MODERESSUSHANLO KH M; PODUGOL'NIKOVA OA; MARINCHEVA GS et al.1981; GENETIKA; ISSN 0016-6758; SUN; DA. 1981; VOL. 17; NO 4; PP. 726-731; ABS. ENG; BIBL. 27 REF.Article

THE QUANTITATIVE ANALYSIS OF POLYMORPHISM ON HUMAN CHROMOSOMES 1, 9, 16 AND Y. I: DESCRIPTION OF INDIVIDUELA KARYOTYPESPODUGOLNIKOVA OA; PARFENOVA IV; SUSHANOLO HM et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 49; NO 3; PP. 243-250; BIBL. 12 REF.Article

CLASSIFICATION OF QH REGIONS IN HUMAN CHROMOSOMES 1, 9, AND 16 BY C-BANDING.PATIL SR; LUBS HA.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 38; NO 1; PP. 35-38; BIBL. 15 REF.Article

A RAPID METHOD FOR IDENTIFICATION OF CONSTITUTIVE HETEROCHROMATIN OF SECONDARY CONSTRICTION REGIONS OF HUMAN CHROMOSOMES 1, 9 AND 16VERMA RS; VED BRAT S; DOSIK H et al.1982; J. HERED.; ISSN 0022-1503; USA; DA. 1982; VOL. 73; NO 1; PP. 74-76; BIBL. 49 REF.Article

EXPLORING THE POTENTIAL OF COMPOUND; FREE-ARM COMBINATIONS OF CHROMOSOME Z IN DROSOPHILA MELANOGASTER FOR INSECT CONTROL AND THE SURVIVAL TO PUPAE OF WHOLE-ARM TRISOMIESFITZ EARLE M; HOLM DG.1978; GENETICS; USA; DA. 1978; VOL. 89; NO 3; PP. 499-510; BIBL. 11 REF.Article

CONSTITUTIONAL CHROMOSOMAL ABERRATION, T(4;12) (Q23;P11), IN A PATIENT WITH PH1 POSITIVE CHRONIC MYELOCYTIC LEUKEMIAGAHRTON G; FRIBERG K; ZECH L et al.1978; HEREDITAS; SWE; DA. 1978; VOL. 89; NO 2; PP. 169-173; BIBL. 19 REF.Article

SINGLE CD BAND IN DICENTRIC TRANSLOCATIONS WITH ONE SUPPRESSED CENTROMEREDANIEL A.1979; HUM. GENET.; DEU; DA. 1979; VOL. 48; NO 1; PP. 85-92; BIBL. 2 P.Article

HETEROCHROMATIN BLOCKS OF CHROMOSOME PAIRS 1, 9 AND 16 AS A "MARKER" FOR HUMAN DIPLOID CELLS WI-38.GARZICIC B; KESEROVIC B; KESEROVIC N et al.1976; J. BIOL. STANDARDIZ.; G.B.; DA. 1976; VOL. 4; NO 4; PP. 367-369; H.T. 1; BIBL. 7 REF.Article

REPORT OF THE COMMITTEE ON THE GENETIC CONSTITUTION OF CHROMOSOMES 2, 3, 4, 5, 7, 8, 10, 11 AND 12BOOTSMA D; RUDDLE FH.1978; CYTOGENET. CELL GENET.; CHE; DA. 1978; VOL. 22; NO 1-6; PP. 74-91; BIBL. 8 P.Conference Paper

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